Canonical Allele Identifier: PA2827967962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216164
ClinVar RCV Id: RCV000198718 RCV000236990 RCV000446409 RCV000766728 RCV003534469 RCV003996975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1440Arg
CA038949
NM_001354898.2:c.4320T>A
CA16030951
NM_001354898.2:c.4318A>C
CA16030957
NM_001354898.2:c.4320T>G